Histochemical stain of skin biopsies showing fatty alcohol oxidizing activity using hexanol as substrate. A. The staining pattern of a control patient.

Slides:



Advertisements
Similar presentations
Metabolism of ganglioside GM2 in GM2 activator-deficient fibroblasts
Advertisements

Unusual late-onset OTC deficiency pedigree demonstrating male-to-female transmission.466 Patient VI-a had multiple episodes of hyperammonemia starting.
A: Population frequency histogram of urinary debrisoquine/4-hydroxydebrisoquine ratios after debrisoquine administration to 258 individuals in a healthy.
One kindred with two GGM patents
Genomic organization of the human cathepsin K gene
A, Diagnosis of clinical severity (mild, moderate, severe) of hemophilia is based on in vitro coagulant activity as shown. B, Distribution of severe and.
Spectrum of different types of human gene mutations logged in Human Gene Mutation Database as of September 13, 1998 ( Source: The.
Advantages of isolated liver transplantation before kidney failure over combined liver-kidney transplantation afterwards. Oxalate excretion: Black line.
Patterns of genetic change in neuroblastomas
Percentile lines for the relationship between insulin sensitivity (SI) and the first-phase insulin response (AIRglucose) based on data from 93 normal subjects.45.
Morphologic appearance of EH skin. Shown is a semithin section (0
Distribution of diagnoses among the nearly 115,000 cases of lymphoid malignancy diagnosed in There are 5400 cases of acute lymphoid leukemia (ALL),
Distribution of diagnoses among the nearly 115,000 cases of lymphoid malignancy diagnosed in There are 5400 cases of acute lymphoid leukemia (ALL),
IX; formation of sphingolipids, sphingosine is synthesised from L-serine and palmitoyl-CoA. Source: Serine deficiency disorders, The Online Metabolic and.
Proposed model for the structure of ABC1 within the plasma membrane (modified from reference202 ). The two symmetric halves consisting of six membrane-spanning.
Illustration of the origin of tubular cysts
Bone x-ray film of GM1 gangliosidosis patients
Light micrographs comparing pycnodysostosis and normal bone
The lymphocyte markers that distinguish the various stages of B-cell differentiation are shown. Markers that are expressed on the cell surface are indicated.
Schematic representation of the DTDST protein
Radiographic appearance of intracranial meningioma in NF2
Agarose gel electrophoresis (A,B,C,D) and two-dimensional nondenaturing polyacrylamide gradient gel electrophoresis (E,F) of plasma from a normolipidemic.
Crystal structure of human short/branched chain acyl-CoA dehydrogenase (PDB file 2JIF). A homotetramer with bound butyryl-Co as substrate is represented.
A section of the cerebellum stained with Sevier-Munger preparation from the brain of a 10-year-old SCA1 patient with 82 CAG repeats who died after 6 years.
Effect of chenodeoxycholic acid feeding on the bilirubin levels of a 10-year-old boy with 3β-hydroxy-Δ5-oxidoreductase/isomerase deficiency. (From Setchell.
Urinary excretion (mg/h) of tryptophan derivatives following administration of oral L-tryptophan (about 70 mg per kilogram body weight) administered to.
Neuropathology. Photomicrographs of the cerebellum
Free energy folding landscape for a hypothetical protein
Translocations predisposing to the occurrence of Down syndrome
Translocations predisposing to the occurrence of Down syndrome
Progressive myopathy in a patient with type IIIa glycogen storage disease. The patient has a debrancher deficiency in both liver and muscle (subtype IIIa).
Diagnostic algorithm for suspected primary myelofibrosis
Model depicting the cycling of REP
Basal and peak serum thyrotropin (TSH) concentrations following intravenous administration of 500 μg thyrotropin-releasing factor (TRF) to subjects with.
Relation between the fractional catabolic rate (FCR) for plasma LDL and the number of LDL receptors on fibroblasts in patients with FH. The values for.
Two children with LPI. The pictures were taken at the time of diagnosis. A, Child 12 years old. B, Child 6 years old. Note the prominent abdomen, hypotrophic.
Evolution of the ubiquitous α-, β-, and γ-crystallins and their structure. Details are described in the text. The α-crystallins are related to heat-shock.
Proton magnetic resonance spectroscopy of the brain of a 5-year-old Japanese boy with SLS. Left panel is T2-weighted MRI showing periventricular white.
Bilateral vestibular schwannoma
Anteroposterior radiographs of right tibia and fibula of case 2 at 2 years of age and left tibia and fibula of case 3 at age 6 years. Features of osteopetrosis.
Mechanism of NO synthesis
A comparison of normal cardiac anatomy (A) and the pathology of hypertrophic cardiomyopathy (B). Hypertrophic cardiomyopathy causes cardiomegaly (570 g;
Orofacial dyskinesia in a patient with Huntington's disease
OCTN2 mRNA in fibroblasts from normal controls and patients with primary carnitine deficiency. PolyA RNA isolated from fibroblasts of normal controls or.
Mechanism of NO synthesis
Insulin secretion rates during graded intravenous glucose infusions administered to 6 MODY-2 subjects with glucokinase (GCK) mutations and 6 control subjects.
Photosensitive skin lesions on the face of a child with C4 deficiency
Expression of mutant human P5C dehydrogenase alleles in yeast
Invasive breast cancer. A
Karyotype of glioblastoma
The renin-angiotensin-aldosterone system
Hydrolysis of membrane-associated ceramide by acid ceramidase in the presence of saposins and bis(monoacylglycero)phosphate (BMP) in the acidic lysosomal.
MRI contrast-enhancement and progression of X-ALD
Key structural elements of p53 DNA binding
Electrophoregram profiles showing the 35delG mutation of CX26 (GJB2) in an individual with recessively inherited hearing loss, and in his heterozygous.
Corneal opacity in a heterozygote observed by slit-lamp microscopy
FISH of glioblastoma. This interphase nucleus from a glioblastoma contains three chromosome 7 centromere signals (dark) and one centromere 10 signal (light).
Young female with OCA1B. The hair was white at birth
Overview of the TGF-β signaling pathway
The effects of apo E alleles on various lipoprotein parameters
Hepatic glucose production as a function of fasting plasma glucose levels. These studies involved the same individuals who were studied in Fig
Basic algorithm for cancer risk assessment that employs gene testing.
Facial features of patients with molybdenum cofactor deficiency [patient 1, top left 4 ; patient 2, top right 117 ; and patient 3, bottom left 83 ] and.
Detection of XIST RNA in interphase cells from a normal male, a normal female, and a 49,XXXXX female by RNA fluorescence in situ hybridization. Male.
Structure and mutation spectrum of BRCA2
Composite megalosaccharide proposed for blood group substance
Complete chemical structures of the neutral glycosphingolipids that accumulate in Fabry disease. A, Globotriaosylceramide, the major accumulated substrate.
Metabolism of mevalonic acid and early steps in the biosynthesis of cholesterol. The structures and names of the intermediates in the synthetic pathway.
The PBDs can be caused by defects in peroxisomal matrix protein import or peroxisome membrane synthesis. Immunofluorescence microscopy shows that human.
DNA analysis on patients with STS deficiency
Presentation transcript:

Histochemical stain of skin biopsies showing fatty alcohol oxidizing activity using hexanol as substrate. A. The staining pattern of a control patient with nonbullous congenital ichthyosis, showing abundant enzyme activity in the basal, spinous, and granular layers. B. Staining pattern of an SLS patient, showing a striking reduction of activity in the spinous and granular layers. Note that some activity is still detectable in the most basal cells, perhaps arising from an alcohol-oxidizing enzyme(s) that is not deficient in SLS. (Dr. Brian Lake, Department of Histopathology, Great Ormond Street Hospital, London, provided this figure.) Source: Sjögren-Larsson Syndrome: Fatty Aldehyde Dehydrogenase Deficiency, The Online Metabolic and Molecular Bases of Inherited Disease Citation: Valle D, Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson K, Mitchell G. The Online Metabolic and Molecular Bases of Inherited Disease; 2014 Available at: https://ommbid.mhmedical.com/DownloadImage.aspx?image=/data/Books/971/ch98fg8.png&sec=62677745&BookID=971&ChapterSecID=62677661&imagename= Accessed: October 14, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved